Results 151 to 160 of about 3,944 (168)

Cardiac involvement in two rare neuromuscular diseases: LAMA2-related muscular dystrophy and SELENON-related myopathy

Neuromuscular Disorders, 2022
Nicol Voermans, Corrie E Erasmus
exaly  

Current Insights Into LAMA2 Disease

2022
openaire   +1 more source

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Frontiers in Molecular Neuroscience, 2020
Anna Sarkozy, Carsten G Bönnemann, Alberto A Zambon   +2 more
exaly   +2 more sources

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Frontiers in Molecular Neuroscience, 2020
Alberto A Zambon, Stefano C. Previtali
exaly  

Muscle magnetic resonance imaging in patients with LAMA2-related muscular dystrophy

Neuromuscular Disorders, 2021
Aijie Liu, Hui Xiong, Haipo Yang
exaly  

Epilepsy in LAMA2-related muscular dystrophy: An electro-clinico-radiological characterization

Epilepsia, 2020
Daniel Natera-de Benito, Pia Gallano, Cecilia Jimenez-Mallebrera   +2 more
exaly  

Phenotypic variability of myopathies associated with LAMA2 gene mutations

European Journal of Paediatric Neurology, 2017
Filipe Palavra, Carmen Costa, Vera Ribeiro, Henriqueta Araújo, Isabel Fineza   +4 more
openaire   +1 more source

LAMA2 gene mutation update: Toward a more comprehensive picture of the laminin-α2 variome and its related phenotypes

Human Mutation, 2018
Mário Sousa, José Pedro Vieira, Ana Gonçalves   +2 more
exaly  

Clinical and molecular genetic analysis of a family with late-onset LAMA2-related muscular dystrophy

Brain and Development, 2016
Juan ding, Renqian Du
exaly  

LAMA2-related myopathy: Frequency among congenital and limb-girdle muscular dystrophies

Muscle and Nerve, 2015
John Vissing, Nicoline Løkken, Morten Duno   +2 more
exaly